Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
NF1	gene	NF1	Expert Review Green;NHS GMS	Neurofibromatosis type 1 (GMS)		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Neurofibromatosis, type 1, OMIM:162200;Neurofibromatosis, familial spinal, OMIM:162210;Neurofibromatosis-Noonan syndrome, OMIM:601321;neurofibromatosis type 1, MONDO:0018975;neurofibromatosis-Noonan syndrome, MONDO:0011035						False	3	100;0;0	1.4	False		ENSG00000196712	ENSG00000196712	HGNC:7765													
SPRED1	gene	SPRED1	Expert Review Green;NHS GMS	Neurofibromatosis type 1 (GMS)		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Legius syndrome, OMIM:611431;Legius syndrome, MONDO:0012669						False	3	100;0;0	1.4	False		ENSG00000166068	ENSG00000166068	HGNC:20249